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  • Homozigotno pomanjkanje alfa 1-antitripsina - prikaz kliničnega primera = Homozygous alpha 1-antitrypsin deficiency - case report
    Kamhi Kiauta, Tina ; Sedmak, Marjeta
    Alpha 1-antitrypsin deficiency is an autosomal recessive disorder. In the article the authors discuss the clinical manifestations, diagnostic proceduresand options for treatment of tlie disease. The ... clinical case of a child, whose alpha 1-antitrypsin deficiency with impaired liver function was discovered after an episode of intracranial haemorrhage in the neonatal period, is presented.
    Vir: Slovenska pediatrija : revija Združenja pediatrov Slovenije in Združenja specialistov šolske in visokošolske medicine Slovenije. - ISSN 1318-4423 (Letn. 11, št. 4, 2004, str. 213-217)
    Vrsta gradiva - članek, sestavni del
    Leto - 2004
    Jezik - slovenski
    COBISS.SI-ID - 19197145

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